Maximilian Cieluch, Norbert Kazamer, Leonard Böhm, Sebastian Sanden, Swen Zerebecki, Florian Wirkert, Ulf–Peter Apfel, Michael Brodmann
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引用次数: 0
Abstract
This study presents the correlation between electrolyte pH, surface morphology, chemical speciation and electro-catalytic oxygen evolution activity of additive-free electrodeposited NiFe catalysts for application in anion exchange membrane water electrolysis. Spherical morphologies were identified at pH 0, shifting towards honey-combed structures at pH 4 with increasing surface area, especially at pH 3. Further, the electrolyte pH was found to influence the NiFe composition and electro-catalytic activity. Enhanced OER activity was noted at pH 2 with overpotentials of 214 mV at 10 mA cm−2 and 267 mV at 100 mA cm−2. The results reveal that the electrolyte pH is a parameter not only influencing the morphology but also tailoring the surface area, Fe oxide and Fe hydroxide composition and consequently the catalytic activity. Further, the outcomes highlight the electrolyte pH as a key process parameter that should be adjusted according to the application, and may substitute the addition of electrolyte-additives, proposing a simpler method for improving catalyst electrodeposition.
研究了无添加剂电沉积NiFe催化剂在阴离子交换膜电解中的应用与电解质pH、表面形貌、化学形态和电催化析氧活性之间的关系。pH值为0时呈球形,pH值为4时随着表面积的增加,尤其是pH值为3时,呈蜂窝状结构。此外,还发现电解液的pH值会影响NiFe的组成和电催化活性。在pH 2下,OER活性增强,在10 mA cm - 2下过电位为214 mV,在100 mA cm - 2下过电位为267 mV。结果表明,电解液的pH值不仅影响催化剂的形貌,而且影响催化剂的表面积、氧化铁和氢氧化铁的组成,从而影响催化剂的催化活性。此外,研究结果强调电解液pH是一个关键的工艺参数,应该根据应用进行调整,并且可以取代电解质添加剂的添加,提出了一种更简单的改善催化剂电沉积的方法。
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.